Electronegatively substituted carboxy-phenyl oxalates as superior chemiluminescent materials

ABSTRACT

NEW COMPOUNDS WHICH ARE REACTIVE WITH HYDROGEN PEROXIDE IN THE PRESENCE OF A SOLVENT AND A FLUORESCER TO PRODUCE VISIBLE CHEMILUMINESCENT LIGHT. THE LIGHT CAPACITY OF THE ELECTRONEGATIVELY SUBSTITUTED CARBOXYPHENYL OXALATE REACTION IS SUPERIOR TO THAT OF THE SIMILARLY ELECTRONEGATIVELY SUBSTITUTED PHENYL OXALATE REACTION.

United States Patent vs. Cl. 260-479 s 4 Claims ABSTRACT OF THE DISCLOSURE New compounds which are reactive with hydrogen peroxide in the presence of a solvent and a fluorescer to produce visible chemiluminescent light. The light capacity of the electronegatively substituted carboxyphenyl oxalate reaction is superior'to that of the similarly electronegatively substituted phenyl oxalate reaction.

This is a division of application Ser. No. 886,406, filed Dec. 18, 1969, now abandoned.

This invention relates to a chemiluminescent light systern using the reaction of an aryl oxalate ester and a peroxide in a diluent in the presence of a fluorescer wherein higher light capacity is obtained by having carboxy substituents on the aryl groups of the oxalate ester.

It has been established by Bollyky and Rauhut, in copending application Ser. No. 619,140, now US. Pat. No. 3,597,362 and elsewhere 1 that superior chemical lighting from the reaction of oxalate esters with fluorescers and hydrogen peroxide, in a diluent, requires an oxalate ester with a high order of reactivity toward hydrogen peroxide. The reactivity of an aromatic ester toward displacement of aromatic phenol by a nucleophile such as hydrogen peroxide can be estimated with substantial accuracy with reference to the Hammett sigma constants of the substituent groups on the displaced aromatic phenol. (See Table .-I for representative Hammett sigma constant values.)

TABLE I Sigma constants for substituent groups in phenols l Ortho Meta Para Group sigma sigma sigma -H 0 0 0 -OCH: 0 0. 08 0. 11 C s 0. 13 -0. 07 0. 17 CH2CH2CH2 -0. 09 0. -0. l3 --CH(CHa)2 0. 23 0. 07 -0. 15 -C(CHa)s 0. 52 0. -0. 20 ---CH: H 0. 0. 08 0. 08 -F 0. 0. 34 0. 06 Cl 0. 0. 37 0.23 -Br 0. 0. 39 0. 27 --NO 1 0. 71 1. 24 -CF| 0. 47 0. 54 -CN 0. 61 0. S8

(3 0. 37 0. 41 t on b 45 0. 37 0. 45 JJOR Data from G. B. Barlin and D. D. Perrin, quart. rev., 20, 75 (1966). Estimated.

Thus, while all oxalate esters are believed to produce detectable light when reacted with hydrogen peroxide, a fluorescer, and, if desired, a basic catalyst, in a diluent L. J. Bollyky, M. Loy, B. G. Roberts, R. H. Whitman. A. V. Iannotta, A. M. Semsel, M. M. Rauhut. Abstracts 153-rd National Meeting of the American Chemical Society, Miami Beach, Fla., April 1967, No. 0-169, M. M. Rauhut, L. J. Bollyky, B. G. Roberts, M. Loy, R. H. Whitman, A V. Iannotta and R. A. Clarke, J. Am. Chem. Soc. 89, 6515 (1967).

the production of superior light intensities from an aromatic oxalate ester requires that the aromatic residue be substituted with sufiicient electronegative substituents to provide a sigma constant sum of at least about 1.4. The values of Hammett sigma constants for a large number of substituents are available in the literature [see for example, G. B. Barlin and D. D. Perrin, Quart. Re., 20, (1966)]. Thus, in general, the structures of superior aromatic oxalate esters are readily predictable.

While H 0 has been indicated as the reactant, it has been also found that hydroperoxide compounds in general will also be effective (as disclosed in copending, commonly assigned US. application Ser. No. 619,140, filed Feb. 28, 1967).

Prior to this invention, however, the light output per unit volume (the light capacity) of oxalate ester chemical lighting systems has been limited by a serious loss of chemiluminescent efiiciency (that is, a reduction in quantum yield) as the concentration of oxalate ester increased. The light capacity is a major criterion for the utility of a chemical lighting system in that the light capacity determines the maximum brightness and useful lifetime of light emission.

Thus the light capacity (L) (in units of lumen hoursliteris related to the brightness and lifetime by:

T: co L=f IdT/V where:

I is the intensity in lumens, T is the time in hours, and V is the volume of the system in liters.

It can be shown that L=4.07 QXCXP where:

Q is the chemiluminescent quantum yield (in units of einsteins per mole of oxalate ester),

C is the concentration of oxalate ester (in units of moles literand P is a photoptic constant which defines the ability of the human eye to see the color of the emitted light.

It is clear from this equation that high light capacities require high quantum yields (Q) at high oxalate concentrations (C), and it is thus readily seen wh'y earlier oxalate ester chemical lighting systems have been limited in light capacity. Thus, at the high oxalate concentrations required for high light capacity, low quantum yields were obtained so that high light capacities were impossible. Indeed, previous oxalate ester chemical light systems have been limited to optimum oxalate ester concentrations below 0.04 M and light capacities have been limited to below about lumen hours liter as in copending, commonly assigned application Ser. No. 813,973, filed Apr. 7, 1969, now abandoned.

It is therefore an object of this invention to provide a chemiluminescent system having a higher light output than those heretofore.

A further object is to provide a method for improving the brightness and useful lifetimes of oxalate ester chemiluminescent systems.

These and other objects of the invention will become apparent as the description thereof proceeds.

I have unexpectedly discovered that the introduction of a carboxy substituent into the aromatic portion of an aryl oxalate substantially reduces the loss in quantum yield obtained with increasing oxalate ester concentration and permits the attainment of high light capacities. This reduction in concentration-derived quantum yield loss obtained by carboxy substitution is limited to substituted phenyl oxalates in which the sum of the Hammett sigma constants of the substituents is less than about 2.7. Thus carboxy phenyl oxalate esters are substituted additionally by other electronegative substituents, so that the sum of all the sigma constants of the substituents lies between 1.4 and about 2.7, provide high quantum yields at high oxalate ester concentrations to give light capacities about 300 lumen hours liter Since the carboxy substituent, which is essential to this result, has a Hammett sigma constant of about 0.9, the sum of the sigma constants of the additional substituents required for high light capacity must be at least about 0.5.

The general class of compounds may be represented by the formula:

OJLELO zq King Y Yn where Xm may represent several different electronegative substituents. Moreover, the aryl oxalate may be additionally substituted by such non-electronegative substituents as alkyl and para-alkoxy, provided only that the sigma sum of all the substituents is at least about 1.4 to 2.7.

Representative carboxyphenyloxalate esters capable of high light capacity are illustrated in Table H.

TABLE II Representative oxalate esters capable of superior light capacities i i Sum of P-OC-COP sigma constants 1 where P-O- is as follows- 1.28 O Bis(2-carboxy-3 4,6-tril (H) chlorophenyljoxalate. Cl- O OH 1.59....: O- Bis(3-carboxy-2 4,6-trichlorophenylioxalate;

1.73 0 Bis(4-carboxy-2,3,6-trichlorophenyDoxalate;

f OH

TAB LE II-C ontinued i if sigma constants 1 where P-O- is as follows- 1.96 O Bis(5-carbalkoxy-3-carboxy- 2,4,6-trich1orophenyl) oxalate.

01- Cl 0 0 R0 C- O 0H 1.65 .1 0 Bis(8-carbalkoxy-2-carboxy- I 4,5,6-trichlorophenyl) C O H oxalate. II 0 Cl C 0 R ll 0 Cl 1.87 0- Bis (4-carbalkoxy-2-carboxy I 3,5,6-trich1orophenyl) oxalate. Ci- 0 OH (I? 0 R O 1.73 O Bis (5-carbalkoxy-2-carboxy- 3,4,6-trichloropheny1) oxalate. Cl O OH 0 \O R 0 C- C1 1.42 O Bis(ti-carbalkoxy-Z-carboxy- 0 O 3,4,5-trichlorophenyl) II II oxalate. R0 O OH 1.92 0-- Bis (2,6-dicarboxy-3 ,4 ,5-

III I ('3' trichlorophenyl) oxalate. H0 0- O OH 1.65 0-- Bis(2,3-dicarboxy-4,5,6-

] O trichlorophenyi) oxalate.

Bis(2,4-dicarboxy-3,4,5-

trichlorophenyl) oxalate.

Bis(2,6-dicarboxy-3,4,6- El) trichlorophenyl) oxalate. Cl- C O H O HO 0 Ci TABLE II-Continued Sum of sigma constants I where P-- is as follows- 1.36 O- Bis(2 carboxy-3,4,6-tri- O chloro-fiethoxyphenyl) II oxalate. Cl O 011 1.21...:...... O- Bls(Z-carboxy-3,4,6-trl- O chloro--methylphenyl) ll oxalate. Cl O OH 1.57 O- Bls(2-carboxy-4,6diehloro- 3-nitro-5-oetylphenyl) ll oxalate. Cl 0 0H 1.29...:..-.1 O Bis[2-carboxy-3,5,6-trl- O ehloro-4(1,1,3,3-tetrall methylbutyDphenyl] 01- O OH oxalate.

HaC CH;

(J H: H!) a 1.28 O- Bls(2earboxy-3,4,5 G-tetra- O fluorophenyl) oxalate. F (30H 1.36 0- Bls(3 4,6-trlbromo-2- I C? carboxyphenyDoxalate; Br O OH Br l.

1.29 O Bis(2,4,5-trlbromo-6- O earboxy-ii-hexadecylll phenyl)oxa1ate. Br- 0 OH iaHza- Br 1 Forsubstituent groups (excluding one carboxy group).

There are a number of variables which influence the chemiluminescent reaction and the amount of light output, light intensity and time of illumination. These are listed as follows:

(1) Oxalate structure,

(2) Oxalate concentration, (3) Fluorescer structure,

(4) Fluorescer concentration, (5) Catalyst structure,

(6) Catalyst concentration,

8 (7) H 0 concentration, (8) Distribution of reactants into components, (9) Selection of solvents for components, and (10) Reaction temperature.

The effect of these variables on the reaction is discussed in subsequent paragraphs.

(1) OXALATE STRUCTURE The oxalate ester of this invention is a bis(phenyl) oxalate ester having the formula:

in which the phenyl groups (P) are substituted by (1) at least one carboxy group of the formula in which (2) the phenyl groups P are substituted by at least two additional substituents selected from the group comprising fluoro, chloro, bromo, cyano, trifluoromethyl, carbalkoxy, nitro, alkoxy, alkoxy methyl, methyl, and higher alkyl, said additional substituents being selected so that the sum of their Hammett sigma constants for phenols lies between about 1.0 and 2.3.

The preferred subclass has the carboxy substituent ortho to the phenolic oxygen.

The preferred species is bis(2,4,5-trichloro-6-carboxyphenyl) oxalate.

(2) OXALATE CONCENTRATION The oxalate concentration in the reacting system may vary widely from 0.01 M to 1.5 M. Preferably, the concentration is 0.03 M to 0.3 M.

(3) FLUORESCER STRUCTURE The fluorescent compounds contemplated herein are numerous; and they may be defined broadly as those which do not readily react on contact with the peroxide employed in this invention, such as hydrogen peroxide; likewise they do not readily react on contact with the ester of oxalic acid. Typical suitable fluorescent compounds for use in the present invention are those which have a spectral emission falling between 330 millimicrons and 1,000 millimicrons and which are at least partially soluble in any of the above diluents, if such diluent is employed. Among these are the conjugated polycyclic aromatic compounds having at least 3 fused rings, such as: anthraceue, substituted anthracene, benzanthracene, phenanthrene, substituted phenanthrene, naphthacene, substituted naphthacene, pentacene, substituted pentacene, perylene, substituted perylene and the like. Typical substituents for all of these are phenyl, lower alkyl, chlorine, bromine, cyano, alkoxy (C -C and other like substituents which do not interfere with the light-generating reaction contemplated in the present chemiluminescent process.

Numerous other fluorescent compounds having the properties given hereinabove are well known in the art. Many of these are fully described in Fluorescence and Phosphorescence, by Peter Pringsheim, Interscience Publishers, Inc., New York, N.Y., 1969. Other fluorescers are described in The Colour Index, 2nd edition, vol. 2, The American Association of Textile Chemists and Colorists, 1956, pp. 2907-2923. While only typical fluorescent compounds are listed hereinabove, the person skilled in the art is fully aware of the fact that this invention is not so restricted, and that numerous other fluorescent compounds having similar properties are contemplated for use herein.

The preferred fluorescers are 9,10-bis(phenylethynyl)- anthracene, l-methoxy 9,10 bis(phenylethynyl)anthracene, 9,10-diphenylanthracene and perylene.

(4) FLUORESCER CONCENTRATION The fluorescer concentration in the reacting system is broadly 0.0002 to 0.03, preferably 0.001 to 0.005.

(5 CATALYST STRUCTURES Catalyst structures include broadly, basic catalysts including amines, hydroxide, alkoxide, carboxylic acid salts and phenolic salts. Preferred are salts of carboxylic acids and phenols whose conjugate acids have pKa values between 1 and 6, as measured in aqueous solution, as in commonly assigned application Ser. No. 813,846 filed Apr. 7, 1969, now abandoned.

Some preferred examples of catalysts are sodium salicylate, tetrabutylammonium salicylate, potassium salicylate, tetrahexylammonium benzoate, benzyltrimethylammonium m-chlorobenzoate. Other catalysts may be dimagnesium ethylenediamine tetraacetate, tetraethyl ammonium stearate, calcium stearate, magnesium stearate, calcium hydroxide, magnesium hydroxide, lithium stearate, triethyl amine, pyridine, piperadine, imidazole, triethylene diamine and potassium trichlorophenoxide.

(6) CATALYST CONCENTRATION The optimum catalyst concentration in the reacting system depends on catalyst structure but, in general, is broadly zero to 0.1 M, preferably zero to 0.01 M.

(7') H 0 CONCENTRATION The H 0 concentration in this reacting system is broadly 0.01 M to 10 M. Preferably, the H 0 concentration is from equal to the oxalate concentration to four times the oxalate concentration.

(8) COMPONENT FORMULATION The order of combining the reactants for obtaining chemiluminescent light is not critical. A reaction and chemiluminescent light could be obtained by combining all necessary materials in the suitable solvent simultaneously or in any order. However, for a practical lighting system or device, the reactants may be formulated as combinations in separate components in such a way that a reaction and a chemiluminescent light do not occur until the separate components are combined. Thus the brightness and lifetime recorded in the tables can 'be obtained by:

1) Mixing separate solutions of each individual reactant in any order, providing there is no undue delay,

(2) Combining the oxalate and fluorescer in a solvent as an oxalate component, combining the H 0 and catalyst in a solvent as a peroxide component, and combining the two components, or

(3) Combining the oxalate component of (2) with H 0 (either dissolved in a solvent or as a pure liquid) and with a catalyst (either dissolved in a solvent or a pure liquid or solid.

Good performance can also be obtained by putting the oxalate and fluorescer in solution or as solids on a substrate and activating with a solution of H 0 and a catalyst (as disclosed in copending, commonly assigned US. application 'Ser. No. 741,517, filed July 1, 1968). Carboxy substituted phenyl oxalates are eminently suitable for this application because they dissolve rapidly in polyether solvents such as diethylene glycol diethyl ethers. In the absence of the carboxy substituent phenyl oxalates dissolve slowly after long stirring in organic solvents. Also the oxalate, fluorescer and catalyst may be combined as solids and the combination either alone or in a substrate can be activated by treating with H 0 in a solvent such as diethylene glycol diethyl ether or dimethylphthalate.

(9) SOLVENTS Solvents for the chemiluminescent components are organic solvents of a number of types, set forth as follows.

(1) Oxalate components in solution:

(a) Ethers and polyethers such a diethylene glycol diethyl ether, diethylene glycol dimethyl ether, ethylene glycol dimethyl ethers;

(b) Broadly, esters such as ethyl acetate, ethyl benzoate, dimethyl phthalate, dibutyl phthalate, dioctyl phthalate, methyl formate, triacetin, diethyl oxalate, and dioctyl ter'ephthalate are examples;

(c) Aromatic hydrocarbons such as benzene, toluene,

ethyl benzene, butylbenzene;

(d) Chlorinated hydrocarbons such as chlorobenzene, odichlorobenzene, m-dichlorobenzene, chloroform, carbon tetrachloride, hexachloroethane, tetrachlorotetrafluoropropane.

Of the solvents, the preferred are diethylene glycol diethyl ether, ethyl benzoate, dibutyl phthalate, and dimethyl phthalate.

(2) Peroxide component containing bases:

Broadly, primary, secondary, and tertiary alcohols such as ethyl, hexyl, Z-ethylhexyl, 2-octanol, cyclohexyl, pinacol, glycerol, 1,3-propylene glycol, tertiary butanol and 3-methyl-3-pentanol are used.

The tertiary alcohols such as t-butyl, 3-methyl-3- pentanol, and 3,6-dimethyl-3-octanol are preferred.

(3) Peroxide components Without catalyst for a 2-component uncatalyzed system for a 3-component system, (fluorescer-i-oxalate) +catalyst+hydrogen peroxide or for systems in which a solid oxalate, a solid fluorescer, and a solid catalyst are combined as a component.

Broadly all of the above alcohols and esters in (9)(1) above may be used. It is preferred to use dimethylphthalate or tertiary alcohols.

( l0) REACTION TEMPERATURE Light intensities increase and lifetimes decrease with increasing temperature. However, temperature is not critical to the emission of light above about 40 C. The oxalates of this invention are superior to any previously known oxalates at all temperatures. The preferred range of operation is about 30 F. to F.

In the examples, quantitative chemiluminescence experiments were carried out in a 1-cm. deep, 3-ml. cylindrical quartz cuvette, positioned vertically at the entrance of a previously described calibrated spectroradiometerfluorirneter. The rear surface of the cuvette was blackened to minimize reflection, and a magnetic stirrer was positioned vertically behind the cuvette to provide rapid mixing. Aliquotes of standardized stock solutions of oxalate ester, hydrogen peroxide, fluorescer, catalyst, and solvent as required were combined in the cuvette using all-glass syringes. Separate stock solutions of individual reactants were generally used, but in some experiments the oxalate ester and fluorescer were combined in a single stock solution or the hydrogen peroxide and catalyst were combined in a single stock solution. No diflerence between these procedures was observed. In most experiments a solvent mixture containing an alcohol was used, and the alcohol component of the mixture was used only for stock solutions of hydrogen peroxide and catalyst,

B G. Roberts and R.

11 since oxalate esters react slowly with alcohols, and ifiuorescers tend to be poorly soluble. The order of rewH mm m Sm mam mom 6555mm a EEE En a a 2. odfi w cosh FhdnH-i we:

mm A

T E 5.5 850 e 3 35 E E o 8 33 mmmbag @2553 23s AoZ azmmewmam26m Horimmso 55.55 5 $32.25 omdoa mo mozmommzmzbqnammo a "nomad.

actant addition was not critical, although hydrogen peroxide and catalyst in that order were generally added last. Rapid mixing was obtained, and the mixing rate was not critical at the rapid stirrer speeds used. The experiments were not thermostated, but the ambient conditions maintained reaction temperatures at 25 C.il C.

The intensity of a 5 m spectral segment located near the spectral maxima was recorded as a function of time using a United Systems Corporation Digitec recorder. Spectra were obtained as previously described 2 and were corrected for intensity decay with time during the spectral determination. The raw spectral and intensity decay data were processed as previously described by a Scientific Data 930 Computer programmed with the calibration data to obtain corrected spectra, absolute spectrally-integrated intensities as a function of time, and quantum yields.

EXAMPLE I Bis(6-carboxy-2,4,5-trichlorophenyl)oxalate (TCAPO) 3,5,-6-trichlorosalicylic acid (12.7 g., 0.05 M.) and 9.3 g. (0.05 m.) of dodecylamine were dissolved in 400 m1. of benzene. The solution was evaporated to dryness under an argon atmosphere to obtain a white solid which was washed with 80 ml. n-hexane to obtain 16.3 g. white product M.P. 118 C.-119 C. This product was dissolved in a mixture of 160 ml. of benzene and 320 ml. of

anhydrous ether. The solution was treated with 3.6 ml. (0.0423 In.) of oxalyl chloride and 10.9 ml. (0.079 m.)

of triethylamine at 25 C. The mixture was stirred for 20 minutes and filtered. The mother liquor was evaporated to dryness, and the residue Was washed successively with 160 ml. of n-hexane, and 300 ml. of boiling benzene to obtain 3.0 g. (14%) of white solid product, M.P. 168.5 C.l69 C.

Analysis.-Calcd. for C H CI O (percent): C, 35.79; H, 0.75; Cl, 39.62. Found (percent): C, 35.99; H, 0.84 Cl, 39.13.

EXAMPLE II Bis(4-carboxy, 2,6-dichlorophenyl)oxalate (CDPO) 652? fin: 6a 33:0 m: vw nm 523.5538 CHURCH 23 no woman 22% 55550 e E H83 3 .6 $2. w m u E 8 5 5. e QBE QE m: :33 8 Hawa e pendant 25 a do: 1232c 322m E H 8 305% H553 Jam m mwnoemsucechazfio 3 53 332 a 495 E c i n e fisse a 3 a 9:09 0 saw a E E Q and sewn: Noieim To a solution of 10.3 g. (0.05 m.) of 2,6-dichloro-4- hydroxy benzoic acid in 200 ml. dry benzene and 600 ml. 45 anhydrous ether, 2.3 ml. (0.027 m.) oxalyl chloride and 6.95 ml. (0.05 m.) triethylamine were added at 25 C. The mixture was stirred for one hour under argon, filtered and the mother liquor was evaporated to dryness to obtain the white solid which was slurried with 400 ml. 50 of ether and filtered to obtain 3.3 g. (28.3%) of product M.P. 250-2 d.

Analysis.Calcd. for C H Cl O (percent): C, 41.06;

H, 1.29; CI, 30.30. Found (percent): C, 41.00; H, 1.86; Cl, 30.14.

EXAMPLE III Quantitative experiments with bis(2,4,5-trichloro-6- carboxyphenyl)oxalate (TCAPO) A series of four experiments in diethylene glycol di- 60 ethyl ether (DEC)-3-methyl-3-pentano1 (3M3P) solution are summarized in Table III. Substantially higher light capacities were obtained from TCAPO than available from trichlorophenyl oxalates containing no carboxy substituent at the best conditions. Under these not optimized conditions, TCAPO produced light capacities up to 305 lumen hours liter- The light emission is brighter and faster in pure DEC than in DEC-containing 25% 3-methy1-3-pentanol, but quantum yield and light capacity are approximately the same. The brightness increased and the light capacity decreased somewhat with increased concentration of the sodium salicylate catalyst.

M. M. Rauhut, B. G. Roberts, and A. M. Semsel, J. Am. Chem. Soc., 88, 3604 (1966).

13 I claim: 1 1. A compound of the formula:

0 0 II I 0c 0 z, z,

Xm I Xm Yn Y,

where X represents a substituent having a Hammett sigma con stant greater than 0;

Y represents a carboxy group;

Z represents a member selected from the group consist ing of hydrogen, alkyl, branched alkyl and alkoxy alkyl, where alkyl chains have from 1 to 16 carbon atoms; and,

m, n and q are integers such that the combined Hammett sigma constant value of the X, Y and Z substituents on each phenyl group is between 1.4 and 2.7, each of said m and n being always at least one.

2. A compound according to claim 1 which is a bis(trichl0ro-6-carboxyphenyl)oxalate.

3. A compound according to claim 3 which is bis(2,4, S-trichloro-6-carboxyphenyl)oxalate.

4. A compound according to claim 1 which is bis(2,6-

10 dichlor0-4-carboxyphenyl)oxalate.

References Cited UNITED STATES PATENTS 2,628,249 2/1953 Bruno 260-475 JAMES A. PATTE-N, Primary Examiner US. Cl. X.R.

UNITED STATES PATENT AND TRADEMARK OFFICE CERTIFICATE OF CORRECTION PATENT N0. 3, 3 9

DATED December 25, 1973 INVENTUMS) Laszlo Joseph Bollyky It is certified that error appears in the above-identified patent and that said Letters Patent is hereby corrected as shown below:

In Column 1, insert the following statement as the second paragraph of the Specification:

The invention herein described was made in the course of or under a contract (Contract No. N6092l-67-C-O2l4) or subcontract thereunder, (or grant) with the Department of the Navy.

Signed and Sealed this Eleventh Day of September, 1990 Attest:

HARRY F. MANBECK, JR.

Attesting Oflicer Commissioner of Patents and Trademarks 

